Canonical Allele Identifier: CA360429321

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90985480A>G , CM000667.2:g.90985480A>G	GRCh38
NC_000005.9:g.90281297A>G , CM000667.1:g.90281297A>G	GRCh37
NC_000005.8:g.90317053A>G	NCBI36
NG_007083.1:g.431681A>G
NG_007083.2:g.461137A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18110A>G MANE Select	NP_115495.3:p.His6037Arg
ENST00000405460.9:c.18110A>G MANE Select	ENSP00000384582.2:p.His6037Arg
NM_032119.3:c.18110A>G	NP_115495.3:p.His6037Arg
NR_003149.1:n.18123A>G
NR_003149.2:n.18126A>G
ENST00000405460.6:c.18110A>G	ENSP00000384582.2:p.His6037Arg
ENST00000425867.2:c.5093A>G	ENSP00000392618.2:p.His1698Arg
ENST00000425867.3:c.7064A>G	ENSP00000392618.3:p.His2355Arg
ENST00000638510.1:n.5377A>G
ENST00000638990.1:c.1322A>G
ENST00000639431.1:c.402A>G	ENSP00000491057.1:n.402A>G
ENST00000639707.1:c.194A>G	ENSP00000492328.1:p.His65Arg
ENST00000639821.1:c.194A>G	ENSP00000492216.1:p.His65Arg
ENST00000640369.1:c.194A>G	ENSP00000491401.1:p.His65Arg
ENST00000640407.1:c.4559A>G	ENSP00000491425.1:n.4559A>G
ENST00000640815.1:c.194A>G	ENSP00000491767.1:p.His65Arg
XM_011543675.1:c.18107A>G	XP_011541977.1:p.His6036Arg
XM_011543676.1:c.18029A>G	XP_011541978.1:p.His6010Arg
XM_011543677.1:c.15413A>G	XP_011541979.1:p.His5138Arg
XM_017009963.2:c.18131A>G	XP_016865452.1:p.His6044Arg
XM_017009964.2:c.18128A>G	XP_016865453.1:p.His6043Arg
XM_017009965.1:c.18128A>G	XP_016865454.1:p.His6043Arg
XM_017009966.2:c.18050A>G	XP_016865455.1:p.His6017Arg
XM_017009967.1:c.18035A>G	XP_016865456.1:p.His6012Arg
XM_017009968.2:c.17951A>G	XP_016865457.1:p.His5984Arg
XM_017009969.2:c.18131A>G	XP_016865458.1:p.His6044Arg
XM_017009972.1:c.11249A>G	XP_016865461.1:p.His3750Arg
XM_017009973.1:c.11228A>G	XP_016865462.1:p.His3743Arg